Abstract
The ubiquitin-proteasome system (UPS) is one of the major mechanisms for protein breakdown in cells, targeting proteins for degradation by enzymatically conjugating them to ubiquitin molecules. Intracellular accumulation of ubiquitin-B+1 (UBB+1), a frameshift mutant of ubiquitin-B, is indicative of a dysfunctional UPS and has been implicated in several disorders, including neurodegenerative disease. UBB+1-expressing transgenic mice display widespread labeling for UBB+1 in brain and exhibit behavioral deficits. Here, we show that UBB+1 is specifically expressed in a subset of parasagittal stripes of Purkinje cells in the cerebellar cortex of a UBB+1-expressing mouse model. This expression pattern is reminiscent of that of the constitutively expressed Purkinje cell antigen HSP25, a small heat shock protein with neuroprotective properties.
Original language | English |
---|---|
Pages (from-to) | 746-750 |
Number of pages | 5 |
Journal | Cerebellum |
Volume | 16 |
Issue number | 3 |
DOIs | |
Publication status | Published - Jun 1 2017 |
Bibliographical note
Funding Information:Acknowledgements The authors would like to thank Dr. Richard Hawkes (University of Calgary, Calgary, AB, Canada) for his generous gift of anti-zebrin II antibody and Dr. Carol Armstrong (Mount Royal University, Calgary, AB, Canada) for advice. FWvL received funding from the Internationale Stiching Alzheimer Onderzoek (ISAO, grant # 06502 and 09514), Hersenstichting Nederland (2008.17 and 15F07.48), IPF 2008, and Van Leersum Foundation KNAW 2011. DAH was supported by an ISAO visiting professorship.
Publisher Copyright:
© 2016, The Author(s).
ASJC Scopus Subject Areas
- Neurology
- Clinical Neurology